Allele Registry

Canonical Allele Identifier: PA110635

Gene: CYP27A1 HGNC NCBI

ClinVar RCV:

RCV000004482

RCV000726759

RCV001252459

ClinVar Variation:

4260

HGVS (amino-acid)	Matching Registered Transcripts
NP_000775.1:p.Arg405Gln	CA340216 NM_000784.4:c.1214G>A